Clinical Research Associate

JR Italy; Trento; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is looking for skilled Clinical Research Associates (CRAs) to join their expanding team. This role is vital for ensuring the timely and high-quality delivery of site monitoring activities, adhering to the Site Monitoring Plan. You will collaborate with a diverse team and contribute to the success of global studies. If you have a background in CRO and a passion for quality in clinical trials, this opportunity offers a dynamic environment where your skills will be valued and developed.

Competenze

• 1-4 years of experience in site monitoring within clinical research.
• Strong knowledge of ICH GCP and clinical trial regulations.

Mansioni

• Deliver on the Site Monitoring Plan ensuring quality and timelines.
• Manage sites to minimize QA audit observations.
• Assist in identifying new potential sites for clinical trials.

Conoscenze

Site Monitoring

Communication Skills

Multitasking

ICH GCP Knowledge

Clinical Trial Regulations

Formazione

Bachelor's Degree in a Scientific Discipline

Master's Degree in a Scientific Discipline

Descrizione del lavoro

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CliniRx CRA Positions - Global Study Support Q1 2025

CliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer permanent opportunities to join us on a global study. Ideally, candidates will have a CRO background with experience across multiple therapeutic areas.

As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models. We support clinical outsourcing for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges, with a presence in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose

We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities

1. Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize QA audit observations.
3. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
4. Continuous Skill Development: Regularly enhance technical and soft skills to improve performance and project outcomes.

Work Relations

• Report to the Manager of Clinical Operations for project, functional, and administrative matters.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added

Your commitment to quality and timeliness is crucial for the successful delivery of projects and overall company success.

Key Success Factors

• Timely, high-quality site monitoring activities.
• Prompt report generation and stakeholder communication.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Strong knowledge of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.